Výsledky vyhledávání - "MESH: Sesquiterpenes"

Characterization of four endophytic fungi as potential consolidated bioprocessing hosts for conversion of lignocellulose into advanced biofuels

Autor: Igor V. Grigoriev, Weihua Wu, John M. Gladden, Sirma Mihaltcheva, Kerrie Barry, Bernard Henrissat, Mary Bao Tran-Gyamfi, Mansi Chovatia, Alan Kuo, Erika Lindquist, Hope Hundley, Ryan W. Davis, Kurt LaButti

Publikováno v: Applied Microbiology and Biotechnology
Applied Microbiology and Biotechnology, Springer Verlag, 2017, 101 (6), pp.2603-2618. ⟨10.1007/s00253-017-8091-1⟩
Applied Microbiology and Biotechnology, 2017, 101 (6), pp.2603-2618. ⟨10.1007/s00253-017-8091-1⟩
Applied Microbiology and Biotechnology, Springer Verlag, 2017, 101 (6), pp.2603-2618. 〈10.1007/s00253-017-8091-1〉

International audience; Recently, several endophytic fungi have been demonstrated to produce volatile organic compounds (VOCs) with properties similar to fossil fuels, called "mycodiesel," while growing on lignocellulosic plant and agricultural resid

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c98a7aafdb8d40a133c65b78d60e895b
https://hal.archives-ouvertes.fr/hal-01802800

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Transcriptional regulation of VCAM-1 expression by tumor necrosis factor-α in human tracheal smooth muscle cells: Involvement of MAPKs, NF-κB, p300, and histone acetylation

Autor: Wei-Ning Lin, Chuen-Mao Yang, Jacques Pouysségur, Jong-Shyan Wang, Shue-Fen Luo, Chih-Chung Lin, Chiang-Wen Lee

Publikováno v: Journal of Cellular Physiology
Journal of Cellular Physiology, Wiley, 2006, 207 (1), pp.174-86. ⟨10.1002/jcp.20549⟩

International audience; Tumor necrosis factor-alpha (TNF-alpha) has been shown to induce the expression of adhesion molecules in airway resident cells and contribute to inflammatory responses. Here, the roles of mitogen-activated protein kinases (MAP

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33ebe757d3d4cb54185033c287208da2
https://doi.org/10.1002/jcp.20549

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Sesquiterpenoids and Cytotoxic Lignans from the Bark of Libocedrus chevalieri

Autor: Thierry Sevenet, Ying-Jun Zhang, Marc Litaudon, Hadjira Bousserouel, Vincent Dumontet, Stéphane Léonce, Marie-Thérèse Martin, Odile Thoison, Françoise Guéritte

Publikováno v: Journal of Natural Products
Journal of Natural Products, American Chemical Society, 2007, 70 (8), pp.1368-70. ⟨10.1021/np070124q⟩

International audience; Investigation of an EtOAc extract of the bark of Libocedrus chevalieri led to the isolation of a new cytotoxic lignan, 5-methoxy-4-epipodophyllotoxin (1), and three known podophyllotoxin analogues, 5-methoxypodophyllotoxin, 5-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42abf9953ffc6da8226d2d02a1d3f420
https://doi.org/10.1021/np070124q

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Correlation of the dynamics of native human acetylcholinesterase and its inhibited huperzine A counterpart from sub-picoseconds to nanoseconds

Autor: Judith Peters, Florian Nachon, Patrick Masson, Marcus Trapp, Moeava Tehei, M M Koza, Martin Weik, Marie Trovaslet, N Martinez

Publikováno v: Journal of the Royal Society Interface
Journal of the Royal Society Interface, the Royal Society, 2014, 11 (97), pp.20140372
Journal of the Royal Society Interface, 2014, 11 (97), pp.20140372

It is a long debated question whether catalytic activities of enzymes, which lie on the millisecond timescale, are possibly already reflected in variations in atomic thermal fluctuations on the pico- to nanosecond timescale. To shed light on this puz

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5371b55cf9a4c8e9e9ca3f2fa7657faa
https://hal.univ-grenoble-alpes.fr/hal-01131840

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Ligand-binding properties of a juvenile hormone receptor, Methoprene-tolerant

Autor: Jan Rynes, Marek Jindra, Keiko Takaki, Thomas Iwema, Jean-Philippe Charles, V. Chandana Epa

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2011, 108, pp.21128-21133. ⟨10.1073/pnas.1116123109⟩
Proceedings of the National Academy of Sciences of the United States of America, 2011, 108 (52), pp.21128-21133. ⟨10.1073/pnas.1116123109⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2011, 108 (52), pp.21128-21133. ⟨10.1073/pnas.1116123109⟩

http://www.pnas.org/; International audience; Juvenile hormone (JH) is a sesquiterpenoid of vital importance for insect development, yet the molecular basis of JH signaling remains obscure, mainly because a bona fide JH receptor has not been identifi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3014498bf3569c1df3609013942b8e2b
https://hal.archives-ouvertes.fr/hal-00824822/file/Ligand_binding_properties.pdf

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Tyrosinase inhibitors and sesquiterpene diglycosides from Guioa villosa

Autor: Abdulmagid Alabdul Magid, Marc Litaudon, Catherine Lavaud, Geoffroy Bontemps, Laurence Voutquenne-Nazabadioko

Publikováno v: Planta Medica
Planta Medica, Georg Thieme Verlag, 2008, 74 (1), pp.55-60. ⟨10.1055/s-2007-993780⟩

International audience; Through a bioassay-guided phytochemical investigation involving mushroom tyrosinase inhibitory activity, seven farnesyl diglycosides ( 1 - 7), five flavonoids ( 8 - 12), one trimeric proanthocyanidin ( 13), two triterpenes ( 1

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c774d2e7915fed8914460841dd20aef8
https://hal.archives-ouvertes.fr/hal-00294816

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Pseudoguanolide sesquiterpene lactones from Veroniopsis caudata and their in vitro antiplasmodial activities

Autor: David Ramanitrahasimbola, Medhi Labaïed, Philippe Rasoanaivo, Voahangy Ramanandraibe, Lengo Mambu, Francois Frappier, Marie-Thérèse Martin, Philippe Grellier, Dina L Rakotondramanana

Publikováno v: Journal of Natural Products
Journal of Natural Products, American Chemical Society, 2005, 68, pp.800-803. ⟨10.1021/np0401866⟩
Journal of Natural Products, American Chemical Society, 2005, 68 (5), pp.800-3. ⟨10.1021/np0401866⟩

Two new helenanolide sesquiterpene lactones, 1 and 2, as well as one known related structure, 11α,13-dihydrohelenalin-[2-(1-hydroxyethyl)acrylate] (3), together with 4′-β-D-O-glucopyranosyl-luteolin and ethyl 2,5-dihydroxycinnamate were isolated

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02089c60b5f84f300bf39fbfbb1756b5
https://hal.archives-ouvertes.fr/hal-00086261

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